LIVIVO - The Search Portal for Life Sciences

zur deutschen Oberfläche wechseln
Advanced search

Search results

Result 1 - 10 of total 49

Search options

  1. Article ; Online: Optimizing machine-learning models for mutagenicity prediction through better feature selection.

    Shinada, Nicolas K / Koyama, Naoki / Ikemori, Megumi / Nishioka, Tomoki / Hitaoka, Seiji / Hakura, Atsushi / Asakura, Shoji / Matsuoka, Yukiko / Palaniappan, Sucheendra K

    Mutagenesis

    2022  Volume 37, Issue 3-4, Page(s) 191–202

    Abstract: Assessing a compound's mutagenicity using machine learning is an important activity in the drug discovery and development process. Traditional methods of mutagenicity detection, such as Ames test, are expensive and time and labor intensive. In this ... ...

    Abstract Assessing a compound's mutagenicity using machine learning is an important activity in the drug discovery and development process. Traditional methods of mutagenicity detection, such as Ames test, are expensive and time and labor intensive. In this context, in silico methods that predict a compound mutagenicity with high accuracy are important. Recently, machine-learning (ML) models are increasingly being proposed to improve the accuracy of mutagenicity prediction. While these models are used in practice, there is further scope to improve the accuracy of these models. We hypothesize that choosing the right features to train the model can further lead to better accuracy. We systematically consider and evaluate a combination of novel structural and molecular features which have the maximal impact on the accuracy of models. We rigorously evaluate these features against multiple classification models (from classical ML models to deep neural network models). The performance of the models was assessed using 5- and 10-fold cross-validation and we show that our approach using the molecule structure, molecular properties, and structural alerts as feature sets successfully outperform the state-of-the-art methods for mutagenicity prediction for the Hansen et al. benchmark dataset with an area under the receiver operating characteristic curve of 0.93. More importantly, our framework shows how combining features could benefit model accuracy improvements.
    MeSH term(s) Mutagens/toxicity ; Mutagens/chemistry ; Machine Learning ; Neural Networks, Computer ; Mutagenesis
    Chemical Substances Mutagens
    Language English
    Publishing date 2022-05-09
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 632903-2
    ISSN 1464-3804 ; 0267-8357
    ISSN (online) 1464-3804
    ISSN 0267-8357
    DOI 10.1093/mutage/geac010
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  2. Article ; Online: Asking the right questions for mutagenicity prediction from BioMedical text.

    Acharya, Sathwik / Shinada, Nicolas K / Koyama, Naoki / Ikemori, Megumi / Nishioka, Tomoki / Hitaoka, Seiji / Hakura, Atsushi / Asakura, Shoji / Matsuoka, Yukiko / Palaniappan, Sucheendra K

    NPJ systems biology and applications

    2023  Volume 9, Issue 1, Page(s) 63

    Abstract: Assessing the mutagenicity of chemicals is an essential task in the drug development process. Usually, databases and other structured sources for AMES mutagenicity exist, which have been carefully and laboriously curated from scientific publications. As ... ...

    Abstract Assessing the mutagenicity of chemicals is an essential task in the drug development process. Usually, databases and other structured sources for AMES mutagenicity exist, which have been carefully and laboriously curated from scientific publications. As knowledge accumulates over time, updating these databases is always an overhead and impractical. In this paper, we first propose the problem of predicting the mutagenicity of chemicals from textual information in scientific publications. More simply, given a chemical and evidence in the natural language form from publications where the mutagenicity of the chemical is described, the goal of the model/algorithm is to predict if it is potentially mutagenic or not. For this, we first construct a golden standard data set and then propose MutaPredBERT, a prediction model fine-tuned on BioLinkBERT based on a question-answering formulation of the problem. We leverage transfer learning and use the help of large transformer-based models to achieve a Macro F1 score of >0.88 even with relatively small data for fine-tuning. Our work establishes the utility of large language models for the construction of structured sources of knowledge bases directly from scientific publications.
    MeSH term(s) Mutagens/toxicity ; Databases, Factual
    Chemical Substances Mutagens
    Language English
    Publishing date 2023-12-18
    Publishing country England
    Document type Journal Article
    ISSN 2056-7189
    ISSN (online) 2056-7189
    DOI 10.1038/s41540-023-00324-2
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  3. Article: Genetic characterization of a novel organoid from human malignant giant-cell tumor.

    Suzuki, Rie / Wakamatsu, Toru / Yoshida, Keiichi / Matsuoka, Yukiko / Takami, Haruna / Nakai, Sho / Tamiya, Hironari / Kakunaga, Shigeki / Yagi, Toshinari / Yoshida, Ken-Ichi / Imura, Yoshinori / Yui, Yoshihiro / Sasagawa, Satoru / Takenaka, Satoshi

    Journal of bone oncology

    2023  Volume 41, Page(s) 100486

    Abstract: Malignant giant-cell tumors are extremely rare bone sarcomas that transform from conventional giant-cell tumors during long periods of treatment. Owing to their rarity, no further analysis of their molecular pathogenesis exists, and thus, no standard ... ...

    Abstract Malignant giant-cell tumors are extremely rare bone sarcomas that transform from conventional giant-cell tumors during long periods of treatment. Owing to their rarity, no further analysis of their molecular pathogenesis exists, and thus, no standard treatment has been established. Recently, organoid culture methods have been highlighted for recapturing the tumor microenvironment, and we have applied the culture methods and succeeded in establishing patient-derived organoids (PDO) of rare sarcomas. This study aimed to investigate the genomic characteristics of our established novel organoids from human malignant giant-cell tumors. At our institute, we treated a patient with malignant giant-cell tumor. The remaining sarcoma specimens after surgical resection were cultured according to the air-liquid interface organoid-culture method. Organoids were xenografted into NOD-scid IL2Rgnull mice. The developed tumors were histologically and genomically analyzed to compare their characteristics with those of the original tumors. Genetic changes over time throughout treatment were analyzed, and the genomic status of the established organoid was confirmed. Organoids from malignant giant-cell tumors could be serially maintained using air-liquid interface organoid-culture methods. The tumors developed in xenografted NOD-scid IL2Rgnull mice. After several repetitions of the process, a patient-derived organoid line from the malignant giant-cell tumor was established. Immunohistochemical analyses and next-generation sequencing revealed that the established organoids lacked the
    Language English
    Publishing date 2023-05-25
    Publishing country Netherlands
    Document type Journal Article
    ISSN 2212-1366
    ISSN 2212-1366
    DOI 10.1016/j.jbo.2023.100486
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  4. Article: Establishment of Organoids From Human Epithelioid Sarcoma With the Air-Liquid Interface Organoid Cultures.

    Wakamatsu, Toru / Ogawa, Hisataka / Yoshida, Keiichi / Matsuoka, Yukiko / Shizuma, Kazuko / Imura, Yoshinori / Tamiya, Hironari / Nakai, Sho / Yagi, Toshinari / Nagata, Shigenori / Yui, Yoshihiro / Sasagawa, Satoru / Takenaka, Satoshi

    Frontiers in oncology

    2022  Volume 12, Page(s) 893592

    Abstract: Background: Although biological resources are essential for basic and preclinical research in the oncological field, those of sarcoma are not sufficient for rapid development of the treatment. So far, some sarcoma cell lines have been established, ... ...

    Abstract Background: Although biological resources are essential for basic and preclinical research in the oncological field, those of sarcoma are not sufficient for rapid development of the treatment. So far, some sarcoma cell lines have been established, however, the success rate was low and the established sarcoma types were frequently biased. Therefore, an efficient culture method is needed to determine the various types of sarcomas. Organoid culture is a 3-dimentional culture method that enables the recapitulation of the tumor microenvironment and the success rate reported is higher than the 2-dimentional culture. The purpose of this study was to report our newly established organoids from human epithelioid sarcoma using the air-liquid interface organoid culture method.
    Methods: We treated 2 patients with epithelioid sarcoma in our institute. The remaining sarcoma specimens after surgical resection were embedded in collagen type 1 gels according to the air-liquid interface organoid culture method. After serial passages, we xenografted the organoids to NOD-scid IL2Rgnull (NSG) mice. Using the developed tumors, we performed histological and genomic analyses to compare the similarities and differences with the original epithelioid sarcoma from the patient.
    Results: Organoids from the epithelioid sarcoma could be serially cultured and maintained in collagen type 1 gels for more than 3 passages. Developed orthotopic tumor xenografts were detected in the NSG mice. After the process was repeated severally, the patient derived organoid lines from the epithelioid sarcoma were established. The established organoids showed loss of integrase interactor 1 expression with polymerase chain reaction and immunohistochemical analyses. The xenografted organoids of the epithelioid sarcoma had histologically similar phenotypes with the original tumor and genetically resembled it to some degree.
    Conclusions: The present study demonstrated 2 novel established organoid models of epithelioid sarcoma, and our organoid models could be used to investigate the molecular pathogenesis and develop a novel treatment.
    Language English
    Publishing date 2022-05-23
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2649216-7
    ISSN 2234-943X
    ISSN 2234-943X
    DOI 10.3389/fonc.2022.893592
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  5. Article ; Online: Modeling and simulation using CellDesigner.

    Matsuoka, Yukiko / Funahashi, Akira / Ghosh, Samik / Kitano, Hiroaki

    Methods in molecular biology (Clifton, N.J.)

    2014  Volume 1164, Page(s) 121–145

    Abstract: In silico modeling and simulation are effective means to understand how the regulatory systems function in life. In this chapter, we explain how to build a model and run the simulation using CellDesigner, adopting the standards such as SBML and SBGN. ...

    Abstract In silico modeling and simulation are effective means to understand how the regulatory systems function in life. In this chapter, we explain how to build a model and run the simulation using CellDesigner, adopting the standards such as SBML and SBGN.
    MeSH term(s) Animals ; Computer Simulation ; Gene Regulatory Networks ; Humans ; Models, Biological ; Models, Genetic ; Software ; Systems Biology ; Transcriptional Activation
    Language English
    Publishing date 2014
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 1940-6029
    ISSN (online) 1940-6029
    DOI 10.1007/978-1-4939-0805-9_11
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  6. Article ; Online: Publisher Correction: LimeMap: a comprehensive map of lipid mediator metabolic pathways.

    Nishi, Akinori / Ohbuchi, Katsuya / Kaifuchi, Noriko / Shimobori, Chika / Kushida, Hirotaka / Yamamoto, Masahiro / Kita, Yoshihiro / Tokuoka, Suzumi M / Yachie, Ayako / Matsuoka, Yukiko / Kitano, Hiroaki

    NPJ systems biology and applications

    2021  Volume 7, Issue 1, Page(s) 16

    Language English
    Publishing date 2021-03-08
    Publishing country England
    Document type Published Erratum
    ISSN 2056-7189
    ISSN (online) 2056-7189
    DOI 10.1038/s41540-021-00174-w
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  7. Article ; Online: LimeMap: a comprehensive map of lipid mediator metabolic pathways.

    Nishi, Akinori / Ohbuchi, Katsuya / Kaifuchi, Noriko / Shimobori, Chika / Kushida, Hirotaka / Yamamoto, Masahiro / Kita, Yoshihiro / Tokuoka, Suzumi M / Yachie, Ayako / Matsuoka, Yukiko / Kitano, Hiroaki

    NPJ systems biology and applications

    2021  Volume 7, Issue 1, Page(s) 6

    Abstract: Lipid mediators are major factors in multiple biological functions and are strongly associated with disease. Recent lipidomics approaches have made it possible to analyze multiple metabolites and the associations of individual lipid mediators. Such ... ...

    Abstract Lipid mediators are major factors in multiple biological functions and are strongly associated with disease. Recent lipidomics approaches have made it possible to analyze multiple metabolites and the associations of individual lipid mediators. Such systematic approaches have enabled us to identify key changes of biological relevance. Against this background, a knowledge-based pathway map of lipid mediators would be useful to visualize and understand the overall interactions of these factors. Here, we have built a precise map of lipid mediator metabolic pathways (LimeMap) to visualize the comprehensive profiles of lipid mediators that change dynamically in various disorders. We constructed the map by focusing on ω-3 and ω-6 fatty acid metabolites and their respective metabolic pathways, with manual curation of referenced information from public databases and relevant studies. Ultimately, LimeMap comprises 282 factors (222 mediators, and 60 enzymes, receptors, and ion channels) and 279 reactions derived from 102 related studies. Users will be able to modify the map and visualize measured data specific to their purposes using CellDesigner and VANTED software. We expect that LimeMap will contribute to elucidating the comprehensive functional relationships and pathways of lipid mediators.
    MeSH term(s) Fatty Acids, Omega-3/metabolism ; Fatty Acids, Omega-6/metabolism ; Humans ; Lipid Metabolism/physiology ; Lipidomics/methods ; Metabolic Networks and Pathways/physiology ; Software ; Systems Biology/methods
    Chemical Substances Fatty Acids, Omega-3 ; Fatty Acids, Omega-6
    Language English
    Publishing date 2021-01-27
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 2056-7189
    ISSN (online) 2056-7189
    DOI 10.1038/s41540-020-00163-5
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  8. Article ; Online: Effects of maoto (ma-huang-tang) on host lipid mediator and transcriptome signature in influenza virus infection.

    Nishi, Akinori / Kaifuchi, Noriko / Shimobori, Chika / Ohbuchi, Katsuya / Iizuka, Seiichi / Sugiyama, Aiko / Ogura, Keisuke / Yamamoto, Masahiro / Kuroki, Haruo / Nabeshima, Shigeki / Yachie, Ayako / Matsuoka, Yukiko / Kitano, Hiroaki

    Scientific reports

    2021  Volume 11, Issue 1, Page(s) 4232

    Abstract: Maoto, a traditional kampo medicine, has been clinically prescribed for influenza infection and is reported to relieve symptoms and tissue damage. In this study, we evaluated the effects of maoto as an herbal multi-compound medicine on host responses in ... ...

    Abstract Maoto, a traditional kampo medicine, has been clinically prescribed for influenza infection and is reported to relieve symptoms and tissue damage. In this study, we evaluated the effects of maoto as an herbal multi-compound medicine on host responses in a mouse model of influenza infection. On the fifth day of oral administration to mice intranasally infected with influenza virus [A/PR/8/34 (H1N1)], maoto significantly improved survival rate, decreased viral titer, and ameliorated the infection-induced phenotype as compared with control mice. Analysis of the lung and plasma transcriptome and lipid mediator metabolite profile showed that maoto altered the profile of lipid mediators derived from ω-6 and ω-3 fatty acids to restore a normal state, and significantly up-regulated the expression of macrophage- and T-cell-related genes. Collectively, these results suggest that maoto regulates the host's inflammatory response by altering the lipid mediator profile and thereby ameliorating the symptoms of influenza.
    MeSH term(s) Animals ; Antiviral Agents ; Disease Models, Animal ; Drugs, Chinese Herbal/administration & dosage ; Ephedra sinica ; Gene Expression Profiling ; Gene Expression Regulation/drug effects ; Host-Pathogen Interactions/genetics ; Host-Pathogen Interactions/immunology ; Humans ; Inflammation Mediators/metabolism ; Influenza A virus ; Influenza, Human/drug therapy ; Influenza, Human/etiology ; Influenza, Human/metabolism ; Macrophages/immunology ; Macrophages/metabolism ; Macrophages/pathology ; Mice ; Orthomyxoviridae Infections/drug therapy ; Orthomyxoviridae Infections/etiology ; Plant Preparations/administration & dosage ; Symptom Assessment ; T-Lymphocytes/drug effects ; T-Lymphocytes/immunology ; T-Lymphocytes/metabolism ; Transcriptome/drug effects ; Viral Load/drug effects
    Chemical Substances Antiviral Agents ; Drugs, Chinese Herbal ; Inflammation Mediators ; Plant Preparations ; Ephedrae herba (51QBA3IQ91)
    Language English
    Publishing date 2021-02-19
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2615211-3
    ISSN 2045-2322 ; 2045-2322
    ISSN (online) 2045-2322
    ISSN 2045-2322
    DOI 10.1038/s41598-021-82707-1
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  9. Article ; Online: Multi-dimensional computational pipeline for large-scale deep screening of compound effect assessment: an in silico case study on ageing-related compounds.

    Gupta, Vipul / Crudu, Alina / Matsuoka, Yukiko / Ghosh, Samik / Rozot, Roger / Marat, Xavier / Jäger, Sibylle / Kitano, Hiroaki / Breton, Lionel

    NPJ systems biology and applications

    2019  Volume 5, Page(s) 42

    Abstract: Designing alternative approaches to efficiently screen chemicals on the efficacy landscape is a challenging yet indispensable task in the current compound profiling methods. Particularly, increasing regulatory restrictions underscore the need to develop ... ...

    Abstract Designing alternative approaches to efficiently screen chemicals on the efficacy landscape is a challenging yet indispensable task in the current compound profiling methods. Particularly, increasing regulatory restrictions underscore the need to develop advanced computational pipelines for efficacy assessment of chemical compounds as alternative means to reduce and/or replace in vivo experiments. Here, we present an innovative computational pipeline for large-scale assessment of chemical compounds by analysing and clustering chemical compounds on the basis of multiple dimensions-structural similarity, binding profiles and their network effects across pathways and molecular interaction maps-to generate testable hypotheses on the pharmacological landscapes as well as identify potential mechanisms of efficacy on phenomenological processes. Further, we elucidate the application of the pipeline on a screen of anti-ageing-related compounds to cluster the candidates based on their structure, docking profile and network effects on fundamental metabolic/molecular pathways associated with the cell vitality, highlighting emergent insights on compounds activities based on the multi-dimensional deep screen pipeline.
    MeSH term(s) Algorithms ; Cluster Analysis ; Computational Biology/methods ; Computer Simulation ; Drug Discovery/methods ; High-Throughput Screening Assays/methods ; Metabolic Networks and Pathways ; Molecular Docking Simulation/methods ; Software
    Language English
    Publishing date 2019-11-26
    Publishing country England
    Document type Journal Article
    ISSN 2056-7189
    ISSN (online) 2056-7189
    DOI 10.1038/s41540-019-0119-y
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  10. Article ; Online: Social engineering for virtual 'big science' in systems biology.

    Kitano, Hiroaki / Ghosh, Samik / Matsuoka, Yukiko

    Nature chemical biology

    2011  Volume 7, Issue 6, Page(s) 323–326

    MeSH term(s) Cooperative Behavior ; Health Personnel/psychology ; Humans ; Science/methods ; Social Behavior ; Systems Biology/methods
    Language English
    Publishing date 2011-05-17
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2202962-X
    ISSN 1552-4469 ; 1552-4450
    ISSN (online) 1552-4469
    ISSN 1552-4450
    DOI 10.1038/nchembio.574
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

To top